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CAS 98-95-3

Nitrobenzene

carcinogenHAPOSHA carcinogendrinking water contaminant

Nitrobenzene smells like bitter almonds and shoe polish — in fact, it was historically used in cheap shoe polish and was the likely cause of multiple poisoning deaths among industrial workers in the 19th century. It is still a major industrial chemical, primarily used to make aniline for polyurethane foam and dyes.

Where It Comes From

Nitrobenzene was first synthesized in 1834 and became widely used as a cheap artificial almond flavoring and shoe polish ingredient in the 19th century, causing documented poisoning deaths in industrial workers who absorbed it through their skin [1]. Today it is primarily an industrial intermediate: most nitrobenzene produced is reduced to aniline, which is then used in polyurethane isocyanate production (for foams in furniture and insulation) and in dye manufacturing [2]. Production facilities are concentrated in major chemical manufacturing regions, and environmental contamination occurs through industrial discharge and spills. Nitrobenzene has contaminated surface water and groundwater near chemical manufacturing facilities. Water from the Jilin City, China chemical plant explosion in 2005 released 100 tons of benzene and nitrobenzene into the Songhua River, a source of drinking water for millions [3].

How You Are Exposed

Occupational inhalation and skin absorption in aniline and dye manufacturing facilities are the primary exposure routes [1]. Nitrobenzene is readily absorbed through skin at room temperature — workers who spill it or handle it without adequate protection develop rapid systemic toxicity. Community exposure occurs near production facilities through air emissions and from contaminated water [2]. Some nail polishes and shoe polishes historically contained nitrobenzene as a solvent or fragrance agent; these uses have largely been discontinued in developed countries [3].

Why It Matters

Nitrobenzene's primary acute toxicity is methemoglobinemia — it oxidizes the iron in hemoglobin from its oxygen-carrying ferrous state to the ferric state that cannot carry oxygen [1]. This produces a characteristic blue-gray skin discoloration (cyanosis) even when blood oxygen levels are not critically low, because methemoglobin causes this color regardless of oxygen. Severe methemoglobinemia causes headache, dizziness, fatigue, shortness of breath, and in high exposures, loss of consciousness and death. Nitrobenzene is also a suspected human carcinogen [2]. The liver is affected by chronic exposures, and animal studies show thyroid, kidney, and bone marrow effects. Methemoglobin is treated with methylene blue given intravenously [3].

Who Is at Risk

Workers in nitrobenzene production, aniline manufacturing, and dye synthesis face the highest occupational risks [1]. Individuals with inherited glucose-6-phosphate dehydrogenase (G6PD) deficiency are more sensitive to nitrobenzene's methemoglobin-forming effects because they have reduced capacity to reverse hemoglobin oxidation [2]. Communities near chemical production facilities with nitrobenzene releases face environmental exposure.

How to Lower Your Exposure

Workers in nitrobenzene environments: wear impermeable chemical gloves, protective clothing, and NIOSH-approved organic vapor respirators — skin absorption is a major route [1]. Regular methemoglobin monitoring (co-oximetry blood test) should be part of occupational health for workers with regular nitrobenzene exposure [2]. For community water contamination near chemical facilities, use certified carbon block or reverse osmosis filters [3].

References

  1. [1]ATSDR. Toxicological Profile for Nitrobenzene. https://www.atsdr.cdc.gov/toxprofiles/tp136.pdf
  2. [2]EPA. Nitrobenzene. https://www.epa.gov/sites/default/files/2016-09/documents/nitrobenzene.pdf
  3. [3]NIOSH. Nitrobenzene. https://www.cdc.gov/niosh/npg/npgd0452.html
  4. [4]Hall AH, Rumack BH. Methemoglobin-forming chemicals. Clin Toxicol. 1994;32(4):411-28.

Recovery & Clinical Information

Body Half-Life

Nitrobenzene is metabolized in the liver to aniline and p-aminophenol — blood half-life is approximately 6-8 hours [1]. Urinary p-nitrophenol and p-aminophenol are metabolites excreted within 24-48 hours [2].

Testing & Biomarkers

Urinary p-aminophenol and methemoglobin level for acute occupational exposure [1]. Methemoglobin percentage on co-oximetry (not captured by standard pulse oximetry) is the critical acute toxicity marker [2].

Interventions

Methylene blue (1-2 mg/kg IV) is the antidote for methemoglobinemia from nitrobenzene poisoning [1]. Fresh air and oxygen supplementation. Remove contaminated clothing; wash skin with soap and water [2]. Industrial controls in aniline/isocyanate manufacturing [1].

Recovery Timeline

Blood nitrobenzene clears within 12-24 hours [1]. Methemoglobinemia typically resolves within 6-24 hours with methylene blue treatment and cessation of exposure [2]. Recovery of normal heme function is complete within 1-2 weeks [1].

Recovery References

  1. [1]ATSDR (2016). Toxicological Profile for Nitrobenzene. https://www.atsdr.cdc.gov/toxprofiles/tp105.pdf
  2. [2]EPA IRIS (1993). Nitrobenzene IRIS. https://iris.epa.gov/ChemicalLanding/&substance_nmbr=0079

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